Differential rescue of the renal and hepatic disease in an autosomal recessive polycystic kidney disease mouse mutant. A new model to study the liver lesion.

Autosomal recessive polycystic kidney disease (ARPKD) is characterized by biliary and renal lesions that produce significant morbidity and mortality. The biliary ductual ectasia and hepatic portal fibrosis associated with ARPKD have not been well studied even though such lesions markedly affect the...

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Detalhes bibliográficos
Main Authors: Yoder, B. K., Richards, W. G., Sommardahl, C., Sweeney, W. E., Michaud, E. J., Wilkinson, J. E., Avner, E. D., Woychik, R. P.
Formato: Artigo
Idioma:Inglês
Publicado em: 1997
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1858312/
https://ncbi.nlm.nih.gov/pubmed/9176412
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